000			a
999			_c16145 _d16145
003			OSt
005			20220201155113.0
008			220201b xxu||||| |||| 00| 0 eng d
040			_aAIKTC-KRRC _cAIKTC-KRRC
100			_915733 _aKadam, Hari K.
245			_aUnique synthesis of isochromenoindolone via reductive-oxidative cyclisation approach
250			_aVol.58(B), Jan.
260			_aNew Delhi _bCSIR _c2021
300			_a104-108p.
520			_aFused heterocyclic compounds are extensively studied in medicinal chemistry due to their promising biological properties such as anticancer, antiviral, antimicrobial activities, etc.1-4 Such compounds also find a resemblance to the constituent structures of important natural products5-9 (Figure 1). Indole and isochromane based heterocyclic structures are found in several medicinally important compounds hence a fused convergent structural motif promises interesting biological properties10-13. Isochromenoindolone is one such compound with probable lead to a new class of bioactive compounds14−17. Anticipating a vast potential for medicinal studies for this compound, we directed our efforts towards developing a simple, efficient and versatile method for synthesis of isochromeno[4,3- b]indol-5(11H)-one.
650		0	_95009 _aGENERAL CHEMISTRY
700			_915734 _aTilve, Santosh G.
773	0		_dNew Delhi NISCAIR-CSIR 2005 _tIndian journal of chemistry (Section B)
856			_uhttp://nopr.niscair.res.in/bitstream/123456789/45703/1/IJCB%2058B%281%29%20104-108.pdf _yClick here
942			_2ddc _cAR